Does CERTOLIZUMAB PEGOL Cause Product dose omission issue? 3,630 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 3,630 reports of Product dose omission issue have been filed in association with CERTOLIZUMAB PEGOL (Cimzia). This represents 3.7% of all adverse event reports for CERTOLIZUMAB PEGOL.
3,630
Reports of Product dose omission issue with CERTOLIZUMAB PEGOL
3.7%
of all CERTOLIZUMAB PEGOL reports
9
Deaths
315
Hospitalizations
How Dangerous Is Product dose omission issue From CERTOLIZUMAB PEGOL?
Of the 3,630 reports, 9 (0.2%) resulted in death, 315 (8.7%) required hospitalization, and 5 (0.1%) were considered life-threatening.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CERTOLIZUMAB PEGOL. However, 3,630 reports have been filed with the FAERS database.
What Other Side Effects Does CERTOLIZUMAB PEGOL Cause?
Drug ineffective (23,838)
Rheumatoid arthritis (17,782)
Pain (13,929)
Fatigue (11,438)
Off label use (10,281)
Rash (9,663)
Alopecia (9,111)
Maternal exposure during pregnancy (9,013)
Arthralgia (8,993)
Abdominal discomfort (8,615)
What Other Drugs Cause Product dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which CERTOLIZUMAB PEGOL Alternatives Have Lower Product dose omission issue Risk?
CERTOLIZUMAB PEGOL vs CERTOPARIN
CERTOLIZUMAB PEGOL vs CETIRIZINE
CERTOLIZUMAB PEGOL vs CETIRIZINE\PSEUDOEPHEDRINE
CERTOLIZUMAB PEGOL vs CETRIMIDE
CERTOLIZUMAB PEGOL vs CETRORELIX